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MECHANISM OF ACTION OF THE SKI ONCOGENE

MECHANISM OF ACTION OF THE SKI ONCOGENE
SKI 癌基因的作用机制
批准号:
6850655
负责人:
MICHAEL John HAYMAN
金额:
$28.61万
依托单位国家:
美国
项目类别:
财政年份:
1986
资助国家:
美国
项目状态:
已结题
起止时间:
1986-05-01 至 2008-02-28

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英文摘要
DESCRIPTION (from the application): Our overall objective is to understand the regulatory mechanisms that control the growth and differentiation of hematopoietic cells in order to understand how oncoproteins subvert these mechanisms to cause leukemia. In this proposal the oncoprotein under study is the v-Ski oncoprotein, which has been demonstrated to cooperate with tyrosine kinases to cause leukemia. Recently the Ski protein has been shown to play a regulatory role in several signal transduction pathways that are frequent targets for mutagenesis in human tumors. Ski interacts with the retinoblastoma protein, (Rb), and effects E2F regulated transcription. It also represses transcription induced by retinoic acid (RA) and by transforming growth factor beta (TGFb). In vitro transformation by Ski is a consequence of over-expression of the Ski protein. This leads to the hypothesis that Ski transforms cells by interacting with complexes involved in signaling by Rb, RA and TGFb and either sequesters important components or disrupts the normal regulatory equilibrium. In vivo Ski plays a role in the causation of hematopoietic stem cell leukemia and mice genetically null for the Ski gene have severe defects in hematopoiesis. These data indicate that Ski plays an important regulatory role in hematopoietic cell growth and differentiation and that these regulatory interactions are important for both normal and malignant hematopoiesis. Our objective is to dissect the role Ski plays in these regulatory pathways and determine how Ski contributes to the causation of hematopoietic malignancies. Our specific aims are: 1. To perform both a genetic and functional analysis of the role of Ski in signaling by nuclear hormone receptors, Rb and TGFb. 2. To dissect the interaction of Ski with the various signaling pathways in hematopoietic cell growth and leukemogenesis. 3. To perform a genetic and functional analysis of the Ski-interacting protein, Skip in the same signaling pathways analyzed for Ski in Aim 1.
期刊论文(47)
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会议论文
Evidence that a cytoplasmically located version of a v-erbB-encoded protein can transform both fibroblasts and erythroblasts.
有证据表明,位于细胞质的 v-erbB 编码蛋白可以转化成纤维细胞和成红细胞。
DOI: 10.1016/0042-6822(92)91253-q
发表时间: 1992
期刊: Virology
影响因子: 3.7
作者: [Lee,EB, Meyer,S, Hayman,MJ]
通讯作者: Hayman,MJ
Common site of mutation in the erbB gene of avian erythroblastosis virus mutants that are temperature sensitive for transformation.
对转化温度敏感的禽成红细胞增多症病毒突变体 erbB 基因的常见突变位点。
DOI: --
发表时间: 1987
期刊: Oncogene research
影响因子: --
作者: [Scotting,P, Vennstrom,B, Jansen,M, Graf,T, Beug,H, Hayman,MJ]
通讯作者: Hayman,MJ
Ski negatively regulates erythroid differentiation through its interaction with GATA1.
Ski 通过与 GATA1 的相互作用负向调节红细胞分化。
DOI: 10.1128/mcb.24.23.10118-10125.2004
发表时间: 2004
期刊: Molecular and cellular biology
影响因子: 5.3
作者: [Ueki,Nobuhide, Zhang,Leiqing, Hayman,MichaelJ]
通讯作者: Hayman,MichaelJ
Avian erythroblastosis: a model system to study oncogene co-operation in leukemia.
禽成红细胞增多症:研究白血病癌基因合作的模型系统。
DOI: --
发表时间: 1992
期刊: Cancer surveys
影响因子: --
作者: [Hayman,MJ, Beug,H]
通讯作者: Beug,H
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